Jointflex

Product NDC: 72927-904
11-digit product format: 729270904
Labeler code: 72927
Product ID: 72927-904_064c9f01-0578-4506-862f-306442181f53
Type: HUMAN OTC DRUG
Nonproprietary name: Jointflex
Dosage form: CREAM
Route: TOPICAL
Labeler: Strides Consumer LLC
Application: M017
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-08-02
Substance: CAMPHOR (SYNTHETIC)
Active strength: 3.2 g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-04	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-03	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72927-904-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-04	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-03	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72927-904-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-04	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-03	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72927-904-01	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Jointflex
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
CAMPHOR (SYNTHETIC)	3.2 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
5TJD82A1ET	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
2181415	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
b82ec69c-bd00-400b-bd94-ac15fb620f9b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
72927-904-01	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-03	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-04	2025-02-07	JointFlex® Pain Relief Cream Drug Facts
72927-904-01	2025-01-30	JointFlex® Pain Relief Cream Drug Facts
72927-904-03	2025-01-30	JointFlex® Pain Relief Cream Drug Facts
72927-904-04	2025-01-30	JointFlex® Pain Relief Cream Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72927-904-01	Jointflex	114 g in 1 TUBE	CREAM	114	5
72927-904-01	Jointflex	1 in 1 CARTON	CREAM	1	5
72927-904-03	Jointflex	1 in 1 CARTON	CREAM	1	5
72927-904-03	Jointflex	28 g in 1 TUBE	CREAM	28	5
72927-904-04	Jointflex	28 g in 1 TUBE	CREAM	28	5
72927-904-04	Jointflex	1 in 1 CARTON	CREAM	1	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72927-904	JOINTFLEX CREAM [STRIDES CONSUMER LLC]	5	Current NDC, Legacy NDC, 6 package rows	20250410_b82ec69c-bd00-400b-bd94-ac15fb620f9b.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 83 of 152 · 3,029 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Chimera GUARD	LIDOCAINE PAIN RELIEFING PATCH	Hangzhou Rongna Health Technology Co., Ltd.	3758d625-010f-7441-e063-6394a90a066d	2025-07-29	Warnings	Exact identifier application number: M017
Cold Therapy Roll on	COLD THERAPY ROLL ON	Allegiant Health	36463acb-7c28-416f-a45f-a93f0be5692b	2025-07-29	Warnings	Exact identifier application number: M017
ProCure Anti Itch	CAMPHOR 0.5%	Twin Med LLC	3afe387c-ef42-215d-e063-6394a90a41b5	2025-07-28	Warnings	Exact identifier application number: M017
lidocaine pain relief patches	LIDOCAINE	Changsha Maocheng Trading Co., Ltd	3afeead3-4f5c-4711-e063-6294a90aacca	2025-07-28	Warnings	Exact identifier application number: M017
SYNC ICE	SYNC RELIEF ICE	iON Pharma, LLC	38ce98ce-a7bf-8041-e063-6394a90ae730	2025-07-28	Warnings	Exact identifier application number: M017
SYNC PRO	SYNC RELIEF PRO CREAM	iON Pharma, LLC	3a3e91d6-732b-dca9-e063-6394a90a06d4	2025-07-28	Warnings	Exact identifier application number: M017
Careland Pain Relief	METHYL SALICYLATE, MENTHOL	Planet (Anhui) Pharmaceutical Co., Ltd.	83f36771-1033-4fd0-a0e6-82c1dcfedeee	2025-07-28	Warnings	Exact identifier application number: M017
Rite Aid anti-itch	HYDROCORTISONE	Rite Aid Corporation	2a232dd1-9071-4c55-a7f7-19d8404b99a6	2025-07-28	Warnings	Exact identifier application number: M017
Hydrocortisone Plus 12 Moisturizers	HYDROCORTISONE	RITE AID CORPORATION	05598255-3e7a-46a5-ae7e-dcfcb616d59d	2025-07-28	Warnings	Exact identifier application number: M017
Inked Inspired	LIDOCAINE HCL	Prodigy Media Inc	54fb2860-7e63-4598-953a-170226e613e9	2025-07-28	Warnings	Exact identifier application number: M017
Ujhay Hydrocortisone Ointment.	UJHAY HYDROCORTISONE OINTMENT	Guangdong Quadrant Ecological Technology Co., Ltd.	3af59276-8e6a-0603-e063-6394a90a1f9b	2025-07-27	Warnings	Exact identifier application number: M017
SANA SANA Menthol External Analgesic	MENTHOL	Alquimia Najulam S de RL de CV	8b7edd51-e08a-4e01-9df0-8305ce17b418	2025-07-25	Warnings	Exact identifier application number: M017
Hydrocortisone Intensive Healing Formula	HYDROCORTISONE	TARGET Corporation	682b737f-e453-4079-bf31-47a9485c7897	2025-07-25	Warnings	Exact identifier application number: M017
Chigg Away	BENZOCAINE	Pierson Laboratories, Inc.	8372e7c1-f145-4bc5-85ab-cf831abe70ce	2025-07-24	Warnings	Exact identifier application number: M017
Chigg Away	BENZOCAINE	Pharma Nobis, LLC	e42fa1c6-d804-630f-e053-2995a90add6b	2025-07-24	Warnings	Exact identifier application number: M017
Cannarelief 2000mg	MENTHOL	Earthmed LLC	01f810de-52ba-8beb-e063-6394a90a61c0	2025-07-24	Warnings	Exact identifier application number: M017
CHING WAN HUNG SOOTHING HERBAL BALM	MENTHOL	TIANJIN DARENTANG JINGWANHONG PHARMACEUTICAL CO., LTD.	ffadc904-8e9d-4cb8-815a-d583bbdb3f0b	2025-07-24	Warnings	Exact identifier application number: M017
PT Elite Premium Pain Relief	CAPSAICIN, MENTHOL	PT ELITE PRODUCTS LLC	ad251821-4c58-425d-bdcb-8dd9bd41b713	2025-07-23	Warnings	Exact identifier application number: M017
Whipped Butter SPF 50	ZINC OXIDE	Bloomeffects, Inc	374b62d8-e012-591f-e063-6294a90aef93	2025-07-23	Warnings	Exact identifier application number: M017
Game On Xtreme	MENTHOL, UNSPECIFIED FORM	Natural Essentials Inc.	5a1b6192-d537-42b3-add8-22c63e7c986c	2025-07-23	Warnings	Exact identifier application number: M017

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5TJD82A1ET	CAMPHOR (SYNTHETIC)	76-22-2	CAMPHOR (SYNTHETIC)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
2181415	camphor 3.2 % Topical Cream	PSN	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5
2181415	camphor 32 MG/ML Topical Cream	SCD	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5
2181415	camphor 3.2 % Topical Cream	SY	b82ec69c-bd00-400b-bd94-ac15fb620f9b	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72927-904-01	72927090401	1 TUBE in 1 CARTON (72927-904-01) / 114 g in 1 TUBE	1 tube	2019-08-02	0000-00-00	No	No	Current
72927-904-03	72927090403	1 TUBE in 1 CARTON (72927-904-03) / 28 g in 1 TUBE	1 tube	2019-08-02		No	No	Current
72927-904-04	72927090404	1 TUBE in 1 CARTON (72927-904-04) / 28 g in 1 TUBE	1 tube	2019-08-02		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
JointFlex® Pain Relief Cream Drug Facts	Strides Consumer LLC \| Beltapharm SPA	2025-04-09	HUMAN OTC DRUG LABEL	5